(19)
(11) EP 0 431 871 A3

(12) EUROPEAN PATENT APPLICATION

(88) Date of publication A3:
06.11.1991 Bulletin 1991/45

(43) Date of publication A2:
12.06.1991 Bulletin 1991/24

(21) Application number: 90313107.6

(22) Date of filing: 03.12.1990
(51) International Patent Classification (IPC)5C07C 221/00
(84) Designated Contracting States:
AT BE CH DE FR GB IT LI NL SE

(30) Priority: 08.12.1989 GB 8927864

(71) Applicant: FINE ORGANICS LIMITED
London WC1B 3RA (GB)

(72) Inventors:
  • Grayson, James Ian
    Western Hill, Durham City, DH1 4BW (GB)
  • Heyes, Graham
    Durham City, DH1 4BW (GB)

(74) Representative: Green, Mark Charles et al
Urquhart-Dykes & Lord, 91 Wimpole Street
London W1M 8AH
London W1M 8AH (GB)


(56) References cited: : 
   
       


    (54) A process for the preparation of ketones


    (57) The present invention relates to the preparation of aminoalkyl p-hydroxyphenyl ketones. Certain of these ketones are well known as important intermediates in the production of compounds having pharmaceutical activity, for example octopamine or synephrine.
    The known Houben-Hoesch reaction is a variation of the Friedel-Crafts reaction and involves the condensation of a phenolic substrate with a nitrile in the presence of a Lewis acid catalyst to give a hydroxy-aryl ketone.
    It is an object of the invention to provide a new or improved process for the manufacture of aminoalkyl p-hydroxyphenyl ketones.
    According to the invention, there is provided a process for the preparation of an aminoalkyl p-hydroxyphenyl ketone comprising reacting phenol with a nitrile, in the presence of a Lewis acid catalyst, to cause condensation thereof, the process being characterised in that the reaction is carried out in a medium comprising a nitroalkane solvent for the reactants.
    A preferred but non-limiting feature of the invention is the productiqn of 2'amino-4-hydroxyacetophenones.
    The present invention is based on the surprising discovery that nitroalkanes are unexpectedly much better solvents for this reaction, being less toxic, giving a better yield and also ensuring a homogeneous reaction medium. The nitroalkanes may also be diluted with a halogenated hydrocarbon solvent, which acts as an inert diluent, thus reducing the amount of nitroalkane used, and making the reaction less hazardous.





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